Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g59780 | A09 | 57740000 | G | A | missense_variant | MODERATE | c.1739C>T|p.Thr580Ile |
S243 |
2 | BAA09g59780 | A09 | 57741849 | G | A | missense_variant | MODERATE | c.926C>T|p.Ala309Val |
S268 |
3 | BAA09g59780 | A09 | 57742093 | C | T | missense_variant | MODERATE | c.746G>A|p.Gly249Glu |
S267 |
4 | BAA09g59780 | A09 | 57742543 | C | T | synonymous_variant | LOW | c.402G>A|p.Glu134Glu |
S67 |
5 | BAA09g59780 | A09 | 57747565 | C | T | upstream_gene_variant | MODIFIER | c.-4621G>A| |
S273 |
6 | BAA09g59780 | A09 | 57747800 | C | T | upstream_gene_variant | MODIFIER | c.-4856G>A| |
S123 |